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AED

NATIONAL ADVANCED ENDOSCOPY DEVICES, INC. · Model 32-4225LA · UDI-DI 00848657084765

FDC Prescription
10
510(k) clearances
444
Adverse events (2 deaths)
0
Recalls
36
Facilities

Description

LASER RESECTOSCOPE WORKING ELEMENT FOR USE WITH 1.5MM LASER FIBERS

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.